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Self-micellizing solid dispersion of thymoquinone with enhanced biopharmaceutical and nephroprotective effects.
Halder, Shimul; Afrose, Sanjida; Shill, Manik Chandra; Sharmin, Nahid; Mollick, Patricia Prova; Shuma, Madhabi Lata; Muhit, Md Abdul; Rahman, S M Abdur.
  • Halder S; Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.
  • Afrose S; Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.
  • Shill MC; Department of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
  • Sharmin N; Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.
  • Mollick PP; Department of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
  • Shuma ML; Department of Pharmacy, School of Pharmacy and Public Health, Independent University Bangladesh, Dhaka, Bangladesh.
  • Muhit MA; Department of Clinical Pharmacy and Pharmacology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.
  • Rahman SMA; Department of Clinical Pharmacy and Pharmacology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh.
Drug Deliv ; 31(1): 2337423, 2024 Dec.
Article en En | MEDLINE | ID: mdl-38590120
ABSTRACT
The present study was designed to develop a self-micellizing solid dispersion (SMSD) containing Thymoquinone (TQM), a phytonutrient obtained from Nigella sativa seeds, aiming to improve its biopharmaceutical and nephroprotective functions. The apparent solubility of TQM in polymer solutions was used to choose an appropriate amphiphilic polymer that could be used to make an SMSD system. Based on the apparent solubility, Soluplus® was selected as an appropriate carrier, and mixing with TQM, SMSD-TQM with different loadings of TQM (5-15%) was made by solvent evaporation and freeze-drying techniques, respectively, and the formulations were optimized. The optimized SMSD-TQM was evaluated in terms of particle size distribution, morphology, release characteristics, pharmacokinetic behavior, and nephroprotective effects in a rat model of acute kidney injury. SMSD-TQM significantly improved the dissolution characteristics (97.8%) of TQM in water within 60 min. Oral administration of SMSD-TQM in rats exhibited a 4.9-fold higher systemic exposure than crystalline TQM. In a cisplatin-induced (6 mg/kg, i.p.) acute kidney-damaged rat model, oral SMSD-TQM (10 mg/kg) improved the nephroprotective effects of TQM based on the results of kidney biomarkers and histological abnormalities. These findings suggest that SMSD-TQM might be efficacious in enhancing the nephroprotective effect of TQM by overcoming biopharmaceutical limitations.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Productos Biológicos / Micelas Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Productos Biológicos / Micelas Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article